| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38374407-38374874 | Rare:185 | ||||
| chr19:38618912-38619332 | Common:3; Rare:117 | ||||
| chr19:38647372-38647825 | Common:3; Rare:152 | ||||
| chr19:38647827-38647907 | Rare:8 | ||||
| chr19:38723607-38724077 | Common:1; Rare:128; Clinvar (benign):2 | ||||
| chr19:38724153-38724565 | Common:2; Rare:137; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:38736971-38737119 | Common:2; Rare:17 | ||||
| chr19:38788962-38789211 | Common:4; Rare:53 | ||||
| chr19:38852315-38852412 | Rare:25 | ||||
| chr19:38878230-38878343 | Rare:17 | ||||
| chr19:38899504-38900047 | Rare:165 | ||||
| chr19:38930737-38931013 | Common:3; Rare:75; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39156417-39156697 | Common:2; Rare:57 | ||||
| chr19:39197104-39197208 | Rare:37 | ||||
| chr19:39197210-39197319 | Rare:29 |